Computer-aided Structural and Molecular Insights into the Mechanisms by which Pseudouridimycin (PUM) Disrupts Cleft Extension in Bacterial RNA Polymerase to Block DNA Entry and Exit

(E-pub Ahead of Print)

Author(s): Ali H. Rabbad, Fisayo A. Olotu, Mahmoud E. Soliman*

Journal Name: Letters in Drug Design & Discovery

Become EABM
Become Reviewer
Call for Editor


Background: The ability of Pseudouridimycin (PUM) to occupy the nucleotide addition site of bacterial RNA Polymerase (RNAP) underlies its inhibitory potency as previously reported. PUM has gained high research interest as a broad-spectrum nucleoside analog that has demonstrated exciting potentials in treating drug-resistant bacterial infections.

Objective: Herein, we identified, for the first time, a novel complementary mechanism by which PUM elicits its inhibitory effects on bacterial RNAP.

Methods: The dynamic binding behavior of PUM to bacterial RNAP was studied using various dynamic analyses approaches.

Results and Discussion: Findings revealed that in addition to occupying the nucleotide addition site, PUM also interrupts the unimpeded entry and exit of DNA by reducing the mechanistic extension of the RNAP cleft and perturbing the primary conformations of the switch regions. Moreover, PUM binding reduced the distances between key residues in the β and β’ subunits that extend to accommodate the DNA.

Conclusion: This study’s findings present structural insights that would contribute to the structure-based design of potent and selective PUM inhibitors.

Keywords: Pseudouridimycin, Nucleoside analog, RNA Polymerase, Switch regions, Cleft extension, Molecular dynamics simulations.

Rights & PermissionsPrintExport Cite as

Article Details

(E-pub Ahead of Print)
DOI: 10.2174/1570180817999201123165144
Price: $95

Article Metrics

PDF: 1